A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15279391



Internal ID5281207
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:68059508..68060467hg38UCSC Ensembl
Innerchr15:68059536..68060439hg38UCSC Ensembl
Outerchr15:68059480..68060495hg38UCSC Ensembl
chr15:68351846..68352805hg19UCSC Ensembl
Innerchr15:68351874..68352777hg19UCSC Ensembl
Outerchr15:68351818..68352833hg19UCSC Ensembl
Cytoband15q23
Allele length
AssemblyAllele length
hg38960
hg19960
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3636800
Supporting Variants
SamplesNA20357
Known GenesPIAS1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15279391
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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